A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104244



Internal ID21287952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4209169..4235365hg38UCSC Ensembl
Innerchr3:4250853..4277049hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3826197
hg1926197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117954
Supporting Variants
Samplessample41
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104244
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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